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Differential
(Click to cross reference)
abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
activities of daily living scale
alpha glucosidase
aneurysm
anterior horn cell disease
aspartate aminotransferase
asymptomatic
calf hypertrophy
cardiomegaly
cardiomyopathy
congestive heart failure
consanguinity
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
delay in diagnosis
developmental retardation
diaphragmatic paralysis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
dyspnea
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
enzyme treatment
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
facial weakness
falling
familial
fatigue
fibrillations
floppy infant
gene
gene mutation
gene therapy
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
hepatomegaly
hip flexor weakness
histochemistry of muscle
hypoglycemia
hypotonia
hypotonia, infants
hypoxia
imbalance
inborn errors of metabolism, screening
ischemic exercise test
leg weakness, bilateral
low back pain
lysosomal storage disease
lysosomes, abnoral
McArdle's disease
misdiagnosis
mortality
MRI, muscle
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
myoglobinuria
myopathy
myopathy, distal, vacuolar
myopathy, genetic
myopathy, metabolic
myopathy, necrotizing
myopathy, vacuolar
myotonic discharges
neck weakness
neurologic disease
neurologic disease, diagnoses of
orthopnea
pain, back
paraspinal muscle
paraspinal muscle weakness
PAS positive
patient in waiting
phosphorylase b kinase deficiency
Pompe's disease of glycogen storage
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
pseudomyotonia
pulmonary function tests
pulmonary hypertension
renal failure
respiratory failure
review article
screening
second wind phenomena
short stature
subarachnoid hemorrhage
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
urine, dark
vital capacity
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
winging of scapula
Showing articles 850 to 900 of 1614 << Previous Next >>

Liver Function Disturbances in Guillain-Barre Syndrome:A Prospective Longitudinal Study in 100 Patients
Neurol 46:96-100, Oomes,P.G.,et al, 1996

Clinicopath Conf
Chronic Schistosoma Mansoni Infection Involving Large Intestine and Spinal Cord, Case 4-1996, NEJM 3, 4:2-389,1996., 1996

Severe Hypoglycaemia and Cognitive Impairment in Diabetes
BMJ 313:767-768, Deary,I.J., 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

Prenatal Magnesium Sulfate Expos/Risk for CP or MR Among Very Low-Birth-Weight Child Aged 3-5 Yrs
JAMA 276:1805-1810, 18431996., Schendel,D.E.,et al, 1996

Riluzole
Lancet 348:795-799, Wokke,J., 1996

A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996

Campylobacter Jejuni Infection and Guillain-Barre Syndrome
NEJM 333:1374-1379, 14151995., Rees,J.H.,et al, 1995

Detection of Borrelia Burgdorferi-Specific Antigen in Antibody-Negative Cerebrospinal Fluid in Neurologic Lyme Disease
Neurol 45:2010-2015, Coyle,P.K.,et al, 1995

The Use of Sumatriptan in Patients with Monoamine Oxidase Inhibitors
Neurol 45:1039-1040, Diamond,S., 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

'Anesthesia Paresthetica':Nitrous Oxide-Induced Cobalamin Deficiency
Neurol 45:1608-1610, 14351995., Kinsella,L.J.&Green,R., 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

Folic Acid and the Prevention of NEural Tube Defects
BMJ 310:1019-1020, Wald,N.J.&Bower,C., 1995

Rapid Antibody Test for Fragile X Syndrome
Lancet 345:1147-1148, Willemsen,R.,et al, 1995

Carbamazepine Hypersensitivity Syndrome:Report of 4 Cases & Review of Literature
Medicine 74:144-151, DeVriese,A.S.P.,et al, 1995

Research Involv Subj with Dementia & Other Cognitive Impairments:NIH, & Ethical Considerations
Neurol 45:1777-1778, Wichman,A.&Sandler,A.L., 1995

Neurologic Abnormalities in Murderers
Neurol 45:1641-1647, Blake,P.Y.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Clinicopath Conf
Intravascular Lymphomatosis, Case 31-1995, NEJM 333:992-999995., , 1995

Systemic Sclerosis Sine Scleroderma:An Unusual Presentation in Scleroderma Renal Crisis
J Rheumatol 22:557-560, Molina,J.F.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Epidemic Optic Neuropathy in Cuba-Clinical Characterization and Risk FActors
NEJM 333:1176-1182, Bern,C.,et al, 1995

Comparison of Therapeutic Effects & Mortality Data of Levodopa & Levodopa with Selegiline in Pts with Early, Mild Parkinson's
BMJ 311:1602-1607, 15831995., Lee,A.J.,et al, 1995

Folate Levels and Neural Tube Defects:Implications for Prevention
JAMA 274:1698-1702, 17171995., Daly,L.E.,et al, 1995

In Utero Exposure to Phenobarbital and Intelligence Deficits in Adult Men
JAMA 274:1518-1525, Reinisch,J.M.,et al, 1995

Anticonvulsant Hypersensitivity Syndrome
Arch Int Med 155:2285-2290, Vittorio,C.C.&Muglia,J.J., 1995

Effects of HIV on Cognitive & Motor Devel in Children Born to HIV-Seropositive Women with no Reported Drug Use:Birth-24 mo
Pediatrics 96:1078-1082, Gay,C.L.,et al, 1995

Plasma Cobalamin Levels Affect Information Processing Speed in a Longitudinal Study of HIV-1 Disease
Arch Neurol 52:195-198, Shor-Posner,G.,et al, 1995

Anterior Communicating Artery Aneurysm Paraparesis Syndrome:Clinical Manifestations and Pathologic Correlates
Neurol 45:45-50, Greene,K.A.,et al, 1995

Association Between Plasma Homocysteine Concentrations and Extracranial Carotid-Artery Stenosis
NEJM 332:286-291, 3281995., Selhub,J.,et al, 1995

Correlation Between CAT Scan Abnormalities & Neuropsychological Function in Children with Symptomatic HIV Disease
Arch Neurol 52:39-44, Brouwers,P.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Neurodevelopmental Outcome of Infants with Hypoplastic Left Heart Syndrome
J Pediatr 126:496-498, Rogers,B.T.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Wernicke Encephalopathy with Symmetric Pericentral Involvement:MR Findings
J Comput Assist Tomogr 19:306-308, Yamashita,M.&Yamamoto,T., 1995

On Politics and Health:An Epidemic of Neurologic Disease in Cuba
Ann Int Med 122:530-533, Roman,G.C., 1995

Gadolinium-Enhanced MR Findings in a Pediatric Case of Wernicke Encephalopathy
AJNR 16:700-702, Harter,S.B.&Nokes,S.R., 1995

Cerebral Venous Thrombosis in Adults:A Study of 40 Cases From Saudi Arabia
Stroke 26:1193-1195, Daif,A.,et al, 1995

Ischemic Stroke as First Manifestation of Essential Thrombocythemia, Report of Six Cases
Stroke 26:1463-1466, Arboix,A.,et al, 1995

Angiotensin-Converting Enzyme Gene Deletion Polymorphism, Risk Factor for Lacune, not Carotid Atheroma
Stroke 26:1329-1333, Markus,H.S.,et al, 1995

Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
Stroke 26:885-890, Simioni,P.,et al, 1995

Serum Folate & Risk for Ischemic Stroke:First Nat'l Health & Nutrition Exam Survey Epidemiologic Follow-Up
Stroke 26:1166-1170, Giles,W.H.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Bilateral Occipital Calcification Associated with Celiac Disease, Folate Deficiency & Epilepsy
AJNR 16:1498-1500, Lea,M.E.,et al, 1995

Cerebrospinal Fluid Concentration of Neuron-specific Enolase in Diagnosis of Creutzfeldt-Jakob Disease
Lancet 345:1609-1610, Zerr,I.,et al, 1995

Dementia Associated with the Acquired Immunodeficiency Syndrome
NEJM 332:934-940, Lipton,S.A.&Gendelman,H.E., 1995

Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
Ann Neurol 38:446-449, Kim,T.W.,et al, 1995

Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
Lancet 345:1260-1264, Tracey,I.,et al, 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995



Showing articles 850 to 900 of 1614 << Previous Next >>